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Cenduit understands the unique needs of the clinical trial supply manager. Your customized IRT (IVRS/IWRS) allows you to control all aspects of drug supply management from creation of the kit list for labeling of the clinical supplies, to confirmation of destruction of drug at the end of the clinical trial.

IRT Drug Supply Management functionalities:

  • Creation of appropriate kit lists for packaging and labeling
  • Technical release of materials at the depots
  • Regulatory release of the materials per country
  • Traceability of manufacturing batches including options to block and recall materials
  • Expiry date management whether the materials were labeled with expiry date or not
  • Expiry date extension and relabeling
  • Flexible depot-to-depot transfer
  • Automated investigator site shipment algorithms that can be adjusted to your study needs throughout the clinical trial
  • Ensuring sufficient stock availability through forecasting different types of clinical supply needs
  • Shipment arrival approval with temperature excursion checks
  • Automated replacement of expiring materials in order to ensure no interruption in clinical supply availability
  • Management of return shipments after drug accountability and reconciliation
  • Tracking destruction of drug at sites or depots
  • Management of ancillary items and lab kits
  • Data integration with sponsor GMP systems, vendor distribution systems, and other eclinical systems
  • Complete visibility of all drug supply data at any time through our custom reporting